Author details

Full Name

Michael Preuss

Affiliation

ORCID

Career Start Year

2009

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
36216889	The contribution of functional HNF1A variants and polygenic susceptibility to risk of type 2 diabetes in ancestrally diverse populations.	Diabetologia	2023
37945903	Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.	Nat Genet	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
38017291	Branched chain amino acids harbor distinct and often opposing effects on health and disease.		2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	2023
37904051	Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.	Nat Genet	2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
36872133	Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry.	Eur Urol	2023
36802703	Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program.	Circulation	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
36865148	: A powerful trans-ancestry Polygenic Risk Score method.		2023
36864090	Effect of tissue-grouped regulatory variants associated to type 2 diabetes in related secondary outcomes.		2023
35085396	Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts.	Diabetes Care	2022
35701873	Genome Wide Association Studies of Variant-by-Thiazide Interaction on Lipids Identifies a Novel Low-Density Lipoprotein Cholesterol Locus.	Circulation Research	2022
35385311	Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.	Sci Adv	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
35399580	Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
36481753	Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.	Nat Commun	2022
34779012	A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.	Genet Epidemiol	2022
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
34376796	Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.	J Hum Genet	2022
34582791	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.	Am J Hum Genet	2021
34108472	Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.	Nat Commun	2021
34107879	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	BMC Genomics	2021
33619380	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Nature Metabolism	2021
34087167	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
33357513	Host genetic effects in pneumonia.	Am J Hum Genet	2021
33137338	Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.	Kidney Int	2021
34521115	Clonal hematopoiesis in sickle cell disease.	Blood	2021
34517814	Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.	BMC Genomics	2021
34604815	Genetic discovery and risk characterization in type 2 diabetes across diverse populations.	HGG Adv	2021
34489608	Prognostic value of polygenic risk scores for adults with psychosis.	Nat Med	2021
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
32692746	The role of polygenic susceptibility to obesity among carriers of pathogenic mutations in MC4R in the UK Biobank population.	PLoS Medicine	2020
32888494	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Cell	2020
31152163	A catalog of genetic loci associated with kidney function from analyses of a million individuals.	Nat Genet	2019
30307499	Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans.	Hum Mol Genet	2019
30084487	Apolipoprotein E gene polymorphisms and intraventricular haemorrhage in infants born preterm: a large prospective multicentre cohort study.	Developmental Medicine and Child Neurology	2019
31491410	Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.	Am J Hum Genet	2019
31217584	Genetic analyses of diverse populations improves discovery for complex traits.	Nature	2019
31118516	Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.	Nature	2019
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018